A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418752



Internal ID21076305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143167601..143203100hg38UCSC Ensembl
chr7:142864694..142900193hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3835500
hg1935500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7156n223
Supporting Variantsnssv18152467
Samples
Known GenesTAS2R39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418752
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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